IRBESARTAN TABLET

Država: Kanada

Jezik: angleščina

Source: Health Canada

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Prenos Lastnosti izdelka (SPC)
02-01-2024

Aktivna sestavina:

IRBESARTAN

Dostopno od:

SIVEM PHARMACEUTICALS ULC

Koda artikla:

C09CA04

INN (mednarodno ime):

IRBESARTAN

Odmerek:

300MG

Farmacevtska oblika:

TABLET

Sestava:

IRBESARTAN 300MG

Pot uporabe:

ORAL

Enote v paketu:

100/500

Tip zastaranja:

Prescription

Terapevtsko območje:

ANGIOTENSIN II RECEPTOR ANTAGONISTS

Povzetek izdelek:

Active ingredient group (AIG) number: 0131700003; AHFS:

Status dovoljenje:

APPROVED

Datum dovoljenje:

2012-05-25

Lastnosti izdelka

                                _IRBESARTAN _
_Page 1 of 37_
_ _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
IRBESARTAN
Irbesartan tablets
Tablets, 75 mg, 150 mg and 300 mg, Oral
USP
Angiotensin II AT
1
Receptor Blocker
Sivem Pharmaceuticals ULC
4705 Dobrin Street
Saint-Laurent, Quebec, Canada
H4R 2P7
www.sivem.ca
Date of Initial Authorization
MAY 25, 2012
Date of revision
JAN 02, 2024
Submission Control No.: 281898
_IRBESARTAN _
_Page 2 of 37_
_ _
RECENT MAJOR LABEL CHANGES
7. WARNINGS AND PRECAUTIONS
01/2024
TABLE OF CONTENTS
RECENT MAJOR LABEL
CHANGES………………………………………………………………………….…...............2
TABLES OF
CONTENTS………………...……………………………………………………………………….…...............2
PART I: HEALTH PROFESSIONAL INFORMATION
.....................................................................
4
1
INDICATIONS
..............................................................................................................
4
1.1
Pediatrics
...................................................................................................................
4
1.2
Geriatrics
...................................................................................................................
4
2
CONTRAINDICATIONS
.................................................................................................
4
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
............................................................ 5
4
DOSAGE AND ADMINISTRATION
.................................................................................
5
4.1
Dosing Considerations
..............................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
......................................................... 5
4.4
Administration
..........................................................................................................
6
4.5
Missed Dose
...............................................
                                
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